• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

microRNAs 在不同疾病状态下的差异表达。

Differential expression of microRNAs in different disease states.

机构信息

Cardiovascular Research Institute, Department of Cell Biology and Molecular Medicine, University of Medicine and Dentistry of New Jersey, Newark, NJ 07103, USA.

出版信息

Circ Res. 2012 Feb 17;110(4):638-50. doi: 10.1161/CIRCRESAHA.111.247437.

DOI:10.1161/CIRCRESAHA.111.247437
PMID:22343558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3324925/
Abstract

Disturbances in gene expression as a result of perturbed transcription or posttranscriptional regulation is one of the main causes of cellular dysfunction that underlies different disease states. Approximately a decade ago, the discovery of microRNAs in mammalian cells has renewed our focus on posttranscriptional regulatory mechanisms during pathogenesis. These tiny posttranscriptional regulators are differentially expressed in almost every disease that has been studied to date and can modulate expression of a gene via specifically binding to its messenger RNA. Because of their capacity to simultaneously target multiple functionally related, genes, they are proving to be potentially powerful therapeutic agents/targets. In this review, we focus on the microRNAs that are differentially regulated in the more common cardiovascular pathologies, their targets, and potential function.

摘要

由于转录或转录后调节受到干扰,导致基因表达紊乱,是导致不同疾病状态下细胞功能障碍的主要原因之一。大约十年前,在哺乳动物细胞中发现 microRNAs,这重新引起了我们对发病机制过程中转录后调控机制的关注。这些微小的转录后调控因子在迄今为止研究过的几乎每种疾病中都有差异表达,并且可以通过特异性结合其信使 RNA 来调节基因的表达。由于它们能够同时针对多个功能相关的基因,因此它们被证明是具有潜在治疗作用的药物/靶点。在这篇综述中,我们重点关注在更常见的心血管病理中差异调节的 microRNAs、它们的靶标以及潜在功能。

相似文献

1
Differential expression of microRNAs in different disease states.microRNAs 在不同疾病状态下的差异表达。
Circ Res. 2012 Feb 17;110(4):638-50. doi: 10.1161/CIRCRESAHA.111.247437.
2
MicroRNAs challenge the status quo of therapeutic targeting.MicroRNAs 挑战治疗靶点的现状。
J Cardiovasc Transl Res. 2009 Mar;2(1):100-7. doi: 10.1007/s12265-008-9052-y. Epub 2008 Sep 9.
3
MicroRNAs: powerful new regulators of heart disease and provocative therapeutic targets.微小RNA:心脏病的强大新型调节因子及具有启发性的治疗靶点。
J Clin Invest. 2007 Sep;117(9):2369-76. doi: 10.1172/JCI33099.
4
MicroRNAs and ultraconserved genes as diagnostic markers and therapeutic targets in cancer and cardiovascular diseases.微小 RNA 和超保守基因作为癌症和心血管疾病的诊断标志物和治疗靶点。
J Cardiovasc Transl Res. 2010 Jun;3(3):271-9. doi: 10.1007/s12265-010-9179-5. Epub 2010 May 5.
5
Expression and function of microRNAs in heart disease.microRNAs 在心脏病中的表达和功能。
Curr Drug Targets. 2010 Aug;11(8):913-25. doi: 10.2174/138945010791591304.
6
Toward microRNA-based therapeutics for heart disease: the sense in antisense.迈向基于微小RNA的心脏病治疗:反义中的意义。
Circ Res. 2008 Oct 24;103(9):919-28. doi: 10.1161/CIRCRESAHA.108.183426.
7
MicroRNAs and cardiac pathology.微小RNA与心脏病理学
Nat Rev Cardiol. 2009 Jun;6(6):419-29. doi: 10.1038/nrcardio.2009.56.
8
MicroRNAs in cardiac remodeling and disease.微小 RNA 在心脏重构和疾病中的作用。
J Cardiovasc Transl Res. 2010 Jun;3(3):212-8. doi: 10.1007/s12265-010-9165-y. Epub 2010 Feb 17.
9
Small engine, big power: microRNAs as regulators of cardiac diseases and regeneration.小引擎,大动力:微小RNA作为心脏疾病和再生的调节因子
Int J Mol Sci. 2014 Sep 9;15(9):15891-911. doi: 10.3390/ijms150915891.
10
MicroRNA control of muscle development and disease.微小RNA对肌肉发育和疾病的调控
Curr Opin Cell Biol. 2009 Jun;21(3):461-9. doi: 10.1016/j.ceb.2009.01.029. Epub 2009 Mar 9.

引用本文的文献

1
From Petri Dish to Primitive Heart: How IVF Alters Early Cardiac Gene Networks and Epigenetic Landscapes.从培养皿到原始心脏:体外受精如何改变早期心脏基因网络和表观遗传格局。
Biomedicines. 2025 Aug 21;13(8):2044. doi: 10.3390/biomedicines13082044.
2
Nobiletin Modulates Adipocyte-Derived Exosomal miRNA to Improve Liver Lipid Metabolism in Obese Mice.诺米林通过调节脂肪细胞衍生的外泌体miRNA改善肥胖小鼠的肝脏脂质代谢。
J Agric Food Chem. 2025 Sep 3;73(35):21959-21975. doi: 10.1021/acs.jafc.5c06392. Epub 2025 Aug 19.
3
Endothelin-1 signaling in the kidney: recent advances and remaining gaps.肾脏中的内皮素-1信号传导:最新进展与尚存差距
Am J Physiol Renal Physiol. 2025 Jun 1;328(6):F815-F827. doi: 10.1152/ajprenal.00304.2024. Epub 2025 Apr 24.
4
ProteotoxomiRs: Diagnostic and pathologic miRNA signatures for reductive stress induced proteotoxic heart disease.蛋白质毒性微小RNA:还原应激诱导的蛋白质毒性心脏病的诊断和病理微小RNA特征
Redox Biol. 2025 Apr;81:103525. doi: 10.1016/j.redox.2025.103525. Epub 2025 Feb 4.
5
Revealing the potential role of hsa-miR-663a in modulating the PI3K-Akt signaling pathway via miRNA microarray in spinal muscular atrophy patient fibroblast-derived iPSCs.揭示 hsa-miR-663a 通过 miRNA 微阵列在脊髓性肌萎缩症患者成纤维细胞衍生的 iPSCs 中调节 PI3K-Akt 信号通路的潜在作用。
J Neuropathol Exp Neurol. 2024 Oct 1;83(10):822-832. doi: 10.1093/jnen/nlae065.
6
Effects of Controlled Ozone Exposure on Circulating microRNAs and Vascular and Coagulation Biomarkers: A Mediation Analysis.受控臭氧暴露对循环微小RNA以及血管和凝血生物标志物的影响:一项中介分析
Noncoding RNA. 2023 Aug 1;9(4):43. doi: 10.3390/ncrna9040043.
7
The Significant Role of microRNAs in Gliomas Angiogenesis: A Particular Focus on Molecular Mechanisms and Opportunities for Clinical Application.微小 RNA 在神经胶质瘤血管生成中的重要作用:特别关注分子机制和临床应用机会。
Cell Mol Neurobiol. 2023 Oct;43(7):3277-3299. doi: 10.1007/s10571-023-01385-x. Epub 2023 Jul 6.
8
miR-802-5p is a key regulator in diabetic kidney disease.微小RNA-802-5p是糖尿病肾病中的关键调节因子。
J Res Med Sci. 2023 May 29;28:43. doi: 10.4103/jrms.jrms_702_22. eCollection 2023.
9
Plasma-derived exosomal miRNA as potential biomarker for diagnosis and prognosis of vector-borne diseases: A review.血浆来源的外泌体微小RNA作为媒介传播疾病诊断和预后的潜在生物标志物:综述
Front Microbiol. 2023 Apr 13;14:1097173. doi: 10.3389/fmicb.2023.1097173. eCollection 2023.
10
ADSC-derived exosomes attenuate myocardial infarction injury by promoting miR-205-mediated cardiac angiogenesis.脂肪间充质干细胞来源的外泌体通过促进 miR-205 介导的心脏血管生成来减轻心肌梗死损伤。
Biol Direct. 2023 Feb 27;18(1):6. doi: 10.1186/s13062-023-00361-1.

本文引用的文献

1
GATA4 expression is primarily regulated via a miR-26b-dependent post-transcriptional mechanism during cardiac hypertrophy.GATA4 的表达主要通过心脏肥大过程中的 miR-26b 依赖的转录后机制进行调控。
Cardiovasc Res. 2012 Mar 15;93(4):645-54. doi: 10.1093/cvr/cvs001. Epub 2012 Jan 4.
2
MicroRNA-1 and -133 increase arrhythmogenesis in heart failure by dissociating phosphatase activity from RyR2 complex.MicroRNA-1 和 -133 通过从 RyR2 复合物上解离磷酸酶活性来增加心力衰竭中的心律失常发生。
PLoS One. 2011;6(12):e28324. doi: 10.1371/journal.pone.0028324. Epub 2011 Dec 6.
3
miR-29b participates in early aneurysm development in Marfan syndrome.miR-29b 参与马凡综合征早期动脉瘤的形成。
Circ Res. 2012 Jan 20;110(2):312-24. doi: 10.1161/CIRCRESAHA.111.253740. Epub 2011 Nov 23.
4
Inhibition of miR-15 protects against cardiac ischemic injury.抑制 miR-15 可预防心脏缺血性损伤。
Circ Res. 2012 Jan 6;110(1):71-81. doi: 10.1161/CIRCRESAHA.111.244442. Epub 2011 Nov 3.
5
Inhibition of miR-33a/b in non-human primates raises plasma HDL and lowers VLDL triglycerides.在非人类灵长类动物中抑制 miR-33a/b 可提高血浆高密度脂蛋白胆固醇并降低极低密度脂蛋白甘油三酯。
Nature. 2011 Oct 19;478(7369):404-7. doi: 10.1038/nature10486.
6
Selective microRNA suppression in human thoracic aneurysms: relationship of miR-29a to aortic size and proteolytic induction.人类胸主动脉瘤中的选择性微小RNA抑制:miR-29a与主动脉大小及蛋白水解诱导的关系
Circ Cardiovasc Genet. 2011 Dec;4(6):605-13. doi: 10.1161/CIRCGENETICS.111.960419. Epub 2011 Oct 18.
7
Novel microRNA prosurvival cocktail for improving engraftment and function of cardiac progenitor cell transplantation.新型 microRNA 生存促进鸡尾酒,改善心脏祖细胞移植的植入和功能。
Circulation. 2011 Sep 13;124(11 Suppl):S27-34. doi: 10.1161/CIRCULATIONAHA.111.017954.
8
MicroRNA-29 in aortic dilation: implications for aneurysm formation.微小 RNA-29 在主动脉扩张中的作用:对动脉瘤形成的影响。
Circ Res. 2011 Oct 28;109(10):1115-9. doi: 10.1161/CIRCRESAHA.111.255737. Epub 2011 Sep 8.
9
Therapeutic inhibition of miR-208a improves cardiac function and survival during heart failure.治疗性抑制 miR-208a 可改善心力衰竭期间的心脏功能和存活率。
Circulation. 2011 Oct 4;124(14):1537-47. doi: 10.1161/CIRCULATIONAHA.111.030932. Epub 2011 Sep 6.
10
Transplantation of human pericyte progenitor cells improves the repair of infarcted heart through activation of an angiogenic program involving micro-RNA-132.人周细胞祖细胞移植通过激活涉及 micro-RNA-132 的血管生成程序改善梗死心脏的修复。
Circ Res. 2011 Sep 30;109(8):894-906. doi: 10.1161/CIRCRESAHA.111.251546. Epub 2011 Aug 25.